Autologous Chondrocyte Implantation in Osteoarthritic Surroundings TNF alpha and Its Inhibition by Adalimumab in a Knee-Specific Bioreactor

作者:Ossendorff Robert; Grad Sibylle; Stoddart Martin J.; Alini Mauro; Schmal Hagen; Sudkamp Norbert; Salzmann Gian M.
来源:The American Journal of Sports Medicine, 2018, 46(2): 431-440.
DOI:10.1177/0363546517737497

摘要

Background: Autologous chondrocyte implantation (ACI) fails in up to 20% of cases. Advanced intra-articular degeneration paired with an inflammatory environment may be closely related to implantation failure. Certain cytokines have been identified to play a major role during early osteoarthritis.
Purpose: To investigate the effects of tumor necrosis factor (TNF) and its potential inhibition by adalimumab on cartilage regeneration in an in vitro model of ACI.
Study Design: Controlled laboratory study.
Methods: Bovine articular chondrocytes were cultivated and transferred at passage 3 to fibrin-polyurethane scaffolds. Constructs were loaded by compression (10%-20% scaffold height) and shear (+/- 25 degrees) in a fully characterized multiaxial load (L) bioreactor to simulate clinical ACI or were subjected to free swelling (FS) conditions for a duration of 2 weeks. TNF alpha (20 ng/mL), adalimumab (10 mu g/mL), or both were added to the medium. To assess the outcome, DNA, GAG (glycosaminoglycan), and total collagen were quantified, and gene expression of anabolic (collagen 2, aggrecan, cartilage oligomeric protein, proteoglycan 4), catabolic (matrix metalloproteinases [MMP] 3 and 13), dedifferentiation (collagen 1), and hypertrophy (collagen 10) markers and proinflammatory cytokines (TNF alpha, IL-1 beta) was analyzed. Histological evaluation was performed with safranin O/fast green, toluidine blue, and immunohistochemistry of collagen 1 and 2. Apoptosis was analyzed by immunolabeling of anti-active caspase 3. For statistical evaluation, nonparametric tests were chosen with a significance level of P < .05.
Results: A general downregulation of anabolic and upregulation of catabolic markers was detected in the TNF alpha groups. Collagen 2 was suppressed by TNF alpha (FS, P = .029; L, P = .006), while MMP 3 was significantly upregulated (FS, P = .035; L, P = .001). Dynamic loading induced a chondrogenic response, which could not fully antagonize the effect of the cytokine. Adalimumab antagonized all effects of TNF alpha. The histological and immunohistochemical assessments demonstrated less matrix formation in the cytokine-only groups. TNF alpha induced apoptosis, and this effect was increased by loading.
Conclusion: TNF does negatively affect chondrogenesis under simulated ACI conditions. Both dynamic load and, more potentially, adalimumab showed the capability of antagonizing the negative effects.

  • 出版日期2018-2